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CIRH1A Protein (Myc-DYKDDDDK Tag)

CIRH1A Origine: Humain Hôte: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
N° du produit ABIN2714195
  • Antigène Voir toutes CIRH1A Protéines
    CIRH1A (Cirrhosis, Autosomal Recessive 1A (Cirhin) (CIRH1A))
    Type de proteíne
    Recombinant
    Origine
    Humain
    Source
    • 2
    • 1
    HEK-293 Cells
    Purification/Conjugué
    Cette CIRH1A protéine est marqué à la Myc-DYKDDDDK Tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Attributs du produit
    • Recombinant human Cirhin protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone
    Pureté
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product CIRH1A Protéine
  • Indications d'application
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Commentaires

    The tag is located at the C-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
    Stock
    -80 °C
    Stockage commentaire
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Antigène
    CIRH1A (Cirrhosis, Autosomal Recessive 1A (Cirhin) (CIRH1A))
    Autre désignation
    Cirhin (CIRH1A Produits)
    Synonymes
    cirhin Protein, Cirhin Protein, Naic Protein, Teg-292 Protein, Tex292 Protein, naic Protein, tex292 Protein, zgc:77199 Protein, wu:fi09g10 Protein, wu:fi37c02 Protein, CIRH1A Protein, CIRHIN Protein, NAIC Protein, TEX292 Protein, UTP4 Protein, UTP4, small subunit processome component Protein, UTP4 small subunit processome component Protein, UTP4 small subunit processome component L homeolog Protein, UTP4 Protein, Utp4 Protein, utp4 Protein, utp4.L Protein
    Sujet
    This gene encodes a WD40-repeat-containing protein that is localized to the nucleolus. Mutation of this gene causes North American Indian childhood cirrhosis, a severe intrahepatic cholestasis that results in transient neonatal jaundice, and progresses to periportal fibrosis and cirrhosis in childhood and adolescence. Alternative splicing results in multiple transcript variants.
    Poids moléculaire
    76.7 kDa
    NCBI Accession
    NP_116219
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